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首页> 外文期刊>Bone marrow transplantation >Infections during mobilizing chemotherapy and following autologous stem cell transplantation.
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Infections during mobilizing chemotherapy and following autologous stem cell transplantation.

机译:动员化疗期间以及自体干细胞移植后的感染。

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Autologous peripheral blood stem cells (PBSC), for transplantation following high-dose chemotherapy, are collected using regimens containing cytokines with or without chemotherapy. The added period of neutropenia prior to stem cell transplantation (SCT) in patients receiving chemotherapy mobilization may increase the risk of infections following transplantation. We studied the incidence of culture-positive infections in 107 consecutive patients who were divided into three groups, according to whether they experienced extended neutropenia during chemotherapy for stem cell mobilization as well as post autotransplant. All the patients received antibiotic prophylaxis and hematopoietic growth factors during neutropenia. The total duration of pre-transplant neutropenia differed among the three mobilization schemes (growth factors alone; one cycle; or two cycles of chemotherapy plus growth factor for mobilization) at 0, 6 and 18 days, respectively (median). However the post-autograft time to myeloid engraftment was similar at 10 days (median). The incidence of culture-proven infections in all three groups was similar. Using fluconazole for yeast prophylaxis, 40% patients developed gastrointestinal colonization with yeast, and the majority of speciated isolates were Candida glabrata. Bacteremia developed in 22% and 9% of patients with S. epidermidis and Gram-negative organisms, respectively, while 11% developed C. difficile-associated diarrhea. In conclusion, treatment using none, one or two cycles of mobilizing chemotherapy pre-transplant does not influence the overall incidence of infections among autologous SCT recipients. However, although post-transplant neutropenia is brief, infections remain a significant cause of morbidity.
机译:大剂量化疗后移植的自体外周血干细胞(PBSC)使用含有细胞因子的方案进行或不进行化疗。在接受化学疗法动员的患者中,干细胞移植(SCT)前中性粒细胞减少的增加期可能会增加移植后感染的风险。我们根据连续干细胞动员化疗和自体移植后是否经历了延长的中性粒细胞减少症,研究了107位连续分为三组的患者的培养阳性感染率。所有患者均在中性粒细胞减少症期间接受了抗生素预防和造血生长因子治疗。在三种动员方案中,移植前中性粒细胞减少的总持续时间(分别为生长因子;一个周期;或两个周期的化疗加动员生长因子)分别在0、6和18天(中位数)有所不同。然而,自体移植后到骨髓移植的时间在10天时相似(中位数)。在所有三个组中,经文化验证的感染的发生率相似。使用氟康唑预防酵母菌,有40%的患者出现了酵母菌在胃肠道的定植,并且大多数标本分离物为光滑念珠菌。表皮葡萄球菌和革兰氏阴性菌患者分别发生细菌血症,占22%和9%,而艰难梭菌相关性腹泻则占11%。总之,在自体SCT接受者中,不进行移植治疗,一次或两个周期动员化疗前的移植治疗不会影响总体感染发生率。然而,尽管移植后中性粒细胞减少是短暂的,但感染仍然是发病的重要原因。

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